WBC Disorders IV Flashcards

1
Q

most common cancer of children

A

acute lymphoblastic leukemia/lymphoma

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2
Q

B-ALLs

A

children - age 3 peak

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3
Q

t(12;21)

A

B-ALL

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4
Q

T-ALLs

A

adolescents peak

-thymic

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5
Q

GOF mutation NOTCH1

A

T-ALL

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6
Q

TdT positive

A

ALLs

-B and T cell

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7
Q

TdT, CD19, CD10, CD20

A

B-ALL

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8
Q

TdT, CD1, CD2, CD5, CD7, CD3, CD4

A

T-ALL

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9
Q

ALL

A

more in boys and whites

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10
Q

hyperdiploidy

A

90% of ALLs

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11
Q

more common ALL

A

B-ALL

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12
Q

B-ALL prognosis

A

aggressive

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13
Q

T-ALL prognosis

A

aggressive

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14
Q

pancytopenia

A

B-ALL

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15
Q

thymic mass and bone marrow involvement

A

T-ALL

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16
Q

ALL clinical

A

abrupt, stormy onset

  • fatigue, fever, bleeding
  • anemia, neutropenia, thrombocytopenia

mass effects - bone pain, lymphademopathy, splenomegaly, hepatomeglay

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17
Q

testicular enlargement

A

ALL

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18
Q

compression of SVC and airways

A

T-ALL

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19
Q

CNS manifestations

A

ALL

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20
Q

ALL and AML

A

very similar clinically
-immunophenotypically distinct

abrupt onset
fever, infection, bleeding
mass effects (more ALL)
CNS sx (more ALL)

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21
Q

most common cause of cancer death in children

A

ALL

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22
Q

favorable ALL prognosis

A
age 2-10
low WBC
hyperdiploidy
trisomy 4, 7, 10
t(12;21)
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23
Q

unfavorable ALL prognosis

A

under age 2
adolescent/adult
peripheral blasts > 100,000
t(9;22) philadelphia

24
Q

philadelphia chromosome

A

t(9;22)

BCR-ABL fusion mutation

25
age 2-10
good ALL prognosis
26
trisomy 4, 7, 10
good ALL prognosis
27
t(12;21)
good ALL prognosis
28
hyperdiploidy
good ALL prognosis
29
CLL vs. SLL
differ only in degree of peripheral blood lymphocytosis | -CLL > 5,000
30
most common leukemia of adults in western world
CLL | -chronic lymphocytic leukemia
31
SLL
small lymphocytic lymphoma
32
dry tap
hairy cell leukemia
33
middle age man with hepatosplenomegaly
hairy cell leukemia
34
CD19/CD20 | CD23/CD5
CLL/SLL
35
deletion 13q, 11q, 17p | trisomy 12q
CLL/SLL
36
fatigable, weight loss, lymphadenopathy, hepatosplenomegaly, small monoclonal Ig spike, hemolytic anemia, hypogammaglobulinemia
CLL/SLL
37
autoantibodies made by nonneoplastic B cells
causes thrombocytopenia in CLL/SLL
38
proliferation centers
pathognomonic for CLL/SLL loose aggregates of larger activated lymphocytes -have mitotically active cells
39
prognosis of SLLC/CLL
indolent
40
CLL/SLL age
around 60yo male often asymptomatic at diagnosis
41
smudge cells
CLL
42
richter syndrome
tranformation of CLL to diffuse large B cell lymphoma - rapidly enlarging mass in node or spleen - survival < 1 year
43
transformation of CLL with prolymphocyte evolution to DLBCL
richter syndrome bad prognosis
44
most common form of indolent NHL in US
follicular lymphoma
45
follicular lymphoma prognosis
indolent - incurable survival 7-9 years
46
BCL2 positive
follicular lymphoma
47
t(14;18)
follicular lymphoma IGH on 14 BCL2 on 18
48
CD19, CD20, CD10, BCL6, BCL2
follicular lymphoma
49
follicular lymphoma
nodular aggregates throughout lymph node | -small centrocytes and large centroblasts
50
spleen in follicular lymphoma
image with lots of white speckles
51
paratrabecular lymphoid aggregates
bone marrow of follicular lymphoma
52
NO CD5
follicular lymphoma
53
peripheral blood in follicular lymphoma
lymphocytosis | -usually < 20,000
54
transformation of follicular lymphoma
30-50% to DLBCL also less commonly to burkitt - myc translocations
55
painless lymphadenopathy, incurable, waxing and waning course, anti-CD20 when symptomatic
follicular lymphoma survival 7-9 years